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Enumerating Viruses by Using Fluorescence and the Nature of the Nonviral Background Fraction

机译:使用荧光枚举病毒和非病毒背景部分的性质

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Bulk fluorescence measurements could be a faster and cheaper way of enumerating viruses than epifluorescence microscopy, flow cytometry, or transmission electron microscopy (TEM). However, since viruses are not imaged, the background fluorescence compromises the signal, and we know little about its nature. In this paper the size ranges of nucleotides that fluoresce in the presence of SYBR gold were determined for wastewater and a range of freshwater samples using a differential filtration method. Fluorescence excitation-emission matrices (FEEMs) showed that >70% of the SYBR fluorescence was in the <10-nm size fraction (background) and was not associated with intact viruses. This was confirmed using TEM. The use of FEEMs to develop a fluorescence-based method for counting viruses is an approach that is fundamentally different from the epifluorescence microscopy technique used for enumerating viruses. This high fluorescence background is currently overlooked, yet it has had a most pervasive influence on the development of a simple fluorescence-based method for quantifying viral abundance in water.
机译:比起荧光显微镜,流式细胞术或透射电子显微镜(TEM),批量荧光测量可能是一种更快,更便宜的枚举病毒的方法。但是,由于未对病毒成像,因此背景荧光会破坏信号,我们对其性质知之甚少。在本文中,使用差动过滤法测定了废水和一系列淡水样品中存在的SYBR金时发出荧光的核苷酸的大小范围。荧光激发-发射矩阵(FEEM)显示,> 70%的SYBR荧光在<10-nm尺寸部分(背景)中,与完整病毒无关。使用TEM证实了这一点。使用FEEM来开发基于荧光的病毒计数方法是一种根本不同于用于枚举病毒的落射荧光显微镜技术的方法。目前忽略了这种高荧光背景,但它对基于简单的基于荧光的定量水中病毒丰度的方法的发展产生了最广泛的影响。

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